Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_assertion description "[The SOS1 E433K mutation, identified in a patient diagnosed with CFC, has previously been reported in patients with NS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_assertion evidence source_evidence_literature NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_assertion SIO_000772 18456719 NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_assertion wasDerivedFrom befree-20140225 NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_assertion wasGeneratedBy ECO_0000203 NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP607445.RA8Kjjor2ZF6GrjO9BWaRnqZTezjXSGs4i7CQho4H0cRA130_provenance.